Autopsy report · NCT03385395
Study Comparing Weekly Intravenous Administration of OctaAlpha1 With a Marketed Preparation Glassia® in Subjects With Alpha-1-antitrypsin Deficiency
Cause of deathRegulatory or ethics
“IND has been closed.”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 2
- Sponsor
- Octapharma
- Sponsor type
- Industry
- Conditions
- Alpha 1-Antitrypsin Deficiency
- Interventions
- OctaAlpha1; Glassia
- Participants
- 0
Trials that died the same way
- Effect of Ulipristal Acetate on Bleeding Patterns and Dysmenorrhea in Women With Adenomyosis
“IND issues” - Phase 1 meCS6 + LT(R192G) Vaccine Study
“IND was terminated for being inactive for more than five years”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.